Long noncoding RNA MARL regulates antiviral responses through suppression miR-122-dependent MAVS downregulation in lower vertebrates

被引:81
|
作者
Chu, Qing [1 ,2 ]
Xu, Tianjun [1 ,2 ,3 ,4 ]
Zheng, Weiwei [1 ,3 ,4 ]
Chang, Renjie [1 ]
Zhang, Lei [1 ]
机构
[1] Shanghai Ocean Univ, Coll Fisheries & Life Sci, Lab Fish Mol Immunol, Shanghai, Peoples R China
[2] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Biol & Biotechnol, Qingdao, Peoples R China
[3] Shanghai Ocean Univ, Natl Pathogen Collect Ctr Aquat Anim, Shanghai, Peoples R China
[4] Shanghai Ocean Univ, Minist Educ, Key Lab Explorat & Utilizat Aquat Genet Resources, Shanghai, Peoples R China
基金
美国国家科学基金会;
关键词
VIRUS-MEDIATED INFLAMMATION; EXPRESSION; PROTEIN; IDENTIFICATION; CONSERVATION; INTERFERONS; ACTIVATION; EVOLUTION; SEQUENCE; PATHWAY;
D O I
10.1371/journal.ppat.1008670
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Increasing evidence suggests important roles for long noncoding RNAs (lncRNAs) as new gene modulators involved in various biological processes. However, the function roles of lncRNAs in lower vertebrates are still unknown. Here, we firstly identify a lncRNA, named MAVS antiviral-related lncRNA (MARL), as a key regulator for antiviral immunity in teleost fish. The results indicate that fish MAVS play essential roles in host antiviral responses and inhibition ofSiniperca chuatsi rhabdovirus(SCRV) replication. miR-122 reduces MAVS expression and suppress MAVS-mediated antiviral responses, which may help viruses evade host antiviral responses. Further, MARL functions as a competing endogenous RNA (ceRNA) for miR-122 to control protein abundance of MAVS, thereby inhibiting SCRV replication and promoting antiviral responses. Our data not only shed new light on understanding the function role of lncRNA in biological processes in lower vertebrates, but confirmed the hypothesis that ceRNA regulatory networks exist widely in vertebrates. Author summary Increasing evidence indicates that lncRNAs participate in the regulation of various biological processes, especially innate and adaptive immunity. However, the relationship between lncRNAs and host antiviral responses remains largely unknown, particularly in lower vertebrates. Our results provided the first direct evidence that a lncRNA, termed MAVS antiviral-related lncRNA (MARL), acts as a key regulator for antiviral immunity in lower vertebrates. lncRNAs has been identified to function as competing endogenous RNAs (ceRNAs) and cross-talk with mRNAs by competing shared for miRNAs. Such ceRNAs regulate the distribution of miRNA molecules on their targets and thereby apply an additional level of post-transcriptional regulation. In our study, MARL functions as a ceRNA for miR-122 to control protein abundance of fish MAVS, thereby inhibiting virus replication and promoting antiviral responses. This is the first study to demonstrate ceRNA regulatory networks existing in lower vertebrates, which can provide new insights into understanding the effects of lncRNAs on host-virus interactions.
引用
收藏
页数:27
相关论文
共 50 条
  • [21] Long noncoding RNA NBAT1 negatively modulates growth and metastasis of osteosarcoma cells through suppression of miR-21
    Yang, Cheng
    Wang, Guijiang
    Yang, Jian
    Wang, Liguo
    AMERICAN JOURNAL OF CANCER RESEARCH, 2017, 7 (10): : 2009 - 2019
  • [22] Downregulation of long noncoding RNA HOTAIRM1 promotes monocyte/dendritic cell differentiation through competitively binding to endogenous miR-3960
    Xin, Jiaxuan
    Li, Jing
    Feng, Yue
    Wang, Liyang
    Zhang, Yuan
    Yang, Rongcun
    ONCOTARGETS AND THERAPY, 2017, 10 : 1 - 9
  • [23] Long noncoding RNA DIO3OS interacts with miR-122 to promote proliferation and invasion of pancreatic cancer cells through upregulating ALDOA
    Kang Cui
    Shuiling Jin
    Yabing Du
    Junlin Yu
    Han Feng
    Qingxia Fan
    Wang Ma
    Cancer Cell International, 19
  • [24] Long noncoding RNA DIO3OS interacts with miR-122 to promote proliferation and invasion of pancreatic cancer cells through upregulating ALDOA
    Cui, Kang
    Jin, Shuiling
    Du, Yabing
    Yu, Junlin
    Feng, Han
    Fan, Qingxia
    Ma, Wang
    CANCER CELL INTERNATIONAL, 2019, 19 (1)
  • [25] Long noncoding RNA NEAT1-modulated miR-506 regulates gastric cancer development through targeting STAT3
    Tan, Hai-Yang
    Wang, Changcheng
    Liu, Gao
    Zhou, Xiang
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2019, 120 (04) : 4827 - 4836
  • [26] Long Noncoding RNA lnc-HC Regulates PPARγ-Mediated Hepatic Lipid Metabolism through miR-130b-3p
    Lan, Xi
    Wu, Litao
    Wu, Nan
    Chen, Qian
    Li, Yue
    Du, Xiaojuan
    Wei, Chenxi
    Feng, Lina
    Li, Yazhao
    Osoro, Ezra Kombo
    Sun, Mengyao
    Ning, Qilan
    Yan, Xiaofei
    Yang, Xudong
    Li, Dongmin
    Lu, Shemin
    MOLECULAR THERAPY-NUCLEIC ACIDS, 2019, 18 : 954 - 965
  • [27] Long noncoding RNA UCA1 regulates HCV replication and antiviral response via miR-145-5p/SOCS7/IFN pathway
    Zeng, Haiyan
    Li, Lei
    Gao, Yi
    Wu, Guojun
    Hou, Zhouhua
    Liu, Shuiping
    INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES, 2021, 17 (11): : 2826 - 2840
  • [28] Long Noncoding RNA GCASPC, a Target of miR-17-3p, Negatively Regulates Pyruvate Carboxylase-Dependent Cell Proliferation in Gallbladder Cancer
    Ma, Ming-zhe
    Zhang, Yan
    Weng, Ming-zhe
    Wang, Shou-hua
    Hu, Ye
    Hou, Zhao-yuan
    Qin, Yi-yu
    Gong, Wei
    Zhang, Yong-Jie
    Kong, Xiang
    Wang, Jian-dong
    Quan, Zhi-wei
    CANCER RESEARCH, 2016, 76 (18) : 5361 - 5371
  • [29] Long noncoding RNA-MEG3 contributes to myocardial ischemia-reperfusion injury through suppression of miR-7-5p expression
    Zou, Liyuan
    Ma, Xiaokun
    Lin, Shuo
    Wu, Bingyuan
    Chen, Yang
    Peng, Chaoquan
    BIOSCIENCE REPORTS, 2019, 39
  • [30] Downregulation of long non-protein coding RNA MVIH impairs glioblastoma cell proliferation and invasion through an miR-302a-dependent mechanism
    Cardoso, Ana M.
    Morais, Catarina M.
    Rebelo, Olinda
    Tao, Herminio
    Barbosa, Marcos
    de Lima, Maria C. Pedroso
    Jurado, Amalia S.
    HUMAN MOLECULAR GENETICS, 2021, 30 (01) : 46 - 64